BBS9
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Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Bardet–Biedl syndrome 9 is a protein that in humans is encoded by the BBS9 gene.[1][2]
The expression of the Bardet–Biedl syndrome 9 protein is downregulated by parathyroid hormone in osteoblastic cells, and therefore, is thought to be involved in parathyroid hormone action in bones.[3]
Mutations in this gene are associated with the Bardet–Biedl syndrome.[2]
References
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External links
[edit | edit source]- Human BBS9 genome location and BBS9 gene details page in the UCSC Genome Browser.
Further reading
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External links
[edit | edit source]- GeneReviews/NIH/NCBI/UW entry on Bardet–Biedl Syndrome
- Bbs9 protein, human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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